Overview

Safety and Efficacy of Bexagliflozin in Subjects With Moderate Hepatic Impairment

Status:
Completed
Trial end date:
2018-12-26
Target enrollment:
Participant gender:
Summary
The purpose of this study is to examine the drug exposure and drug effects on subjects with moderate hepatic impairment after a single oral dose of bexagliflozin tablets, 20mg. The study will also evaluate how safe the study drug is and how well the study drug is tolerated in subjects with moderate hepatic impairment.
Phase:
Phase 1
Details
Lead Sponsor:
Theracos
Treatments:
Bexagliflozin